Who is sponsoring NCT07115225?

NCT07115225 is sponsored by University Ghent.

What drugs are being tested in NCT07115225?

Interventions in NCT07115225: Analytical test - Shoulder Range of Motion (ROM), Analytical test - Shoulder Strength, Modified-Athletic Shoulder Test (M-AST), Physical performance test - Unilateral Seated Shot-Put Test (USSPT), Physical performance test - modified-Closed Kinetic Chain Upper Extremity Stability Test (m-CKCUEST), Supine moving apprehension test (SMAT), Physical performance test - Posterior shoulder endurance test (PSET), Patient-reported outcome measure - The Shoulder Instability-Return to Sport after Injury (SIRSI), Patient-reported outcome measure - Numeric Pain Rating Scale (NPRS), Modified Tampa-Scale of Kinesiophobia for Anterior Shoulder Instability (TSK-SI).

What condition does NCT07115225 study?

NCT07115225 studies Return to Sport, Shoulder Dislocation or Subluxation.

Is NCT07115225 still recruiting?

NCT07115225 is currently recruiting now. Last updated 11 August 2025.

Last reviewed 2025-08-11 · How we verify

NCT07115225: VAL_PPT_P

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Validation of an Upper Extremity Physical Performance Test Battery in Patients After Shoulder Dislocation

Recruiting now NA Last updated 11 August 2025

What this trial tests

NA trial testing Analytical test - Shoulder Range of Motion (ROM) in Return to Sport in 129 participants. Currently enrolling.

Timeline

3 July 2025

Primary endpoint
1 January 2029

1 January 2029

Quick facts

Lead sponsor	University Ghent
Phase	NA
Status	Recruiting now
Study type	INTERVENTIONAL
Allocation	na
Design	single group
Masking	none
Primary purpose	other
Enrollment	129
Start date	3 July 2025
Primary completion	1 January 2029
Estimated completion	1 January 2029
Sites	2 locations across Belgium

Drugs / interventions tested

Analytical test - Shoulder Range of Motion (ROM)
Analytical test - Shoulder Strength
Modified-Athletic Shoulder Test (M-AST)
Physical performance test - Unilateral Seated Shot-Put Test (USSPT)
Physical performance test - modified-Closed Kinetic Chain Upper Extremity Stability Test (m-CKCUEST)
Supine moving apprehension test (SMAT)
Physical performance test - Posterior shoulder endurance test (PSET)
Patient-reported outcome measure - The Shoulder Instability-Return to Sport after Injury (SIRSI)
Patient-reported outcome measure - Numeric Pain Rating Scale (NPRS)
Modified Tampa-Scale of Kinesiophobia for Anterior Shoulder Instability (TSK-SI)

Conditions studied

Return to Sport — all drugs for Return to Sport →
Shoulder Dislocation or Subluxation — all drugs for Shoulder Dislocation or Subluxation →

Sponsor

University Ghent

Who can join

Adults 16 to 55, any sex, with Return to Sport or Shoulder Dislocation or Subluxation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this exploratory prospective study is to determine if an upper extremity test battery, comprised of physical performance tests, analytical tests and patient-reported outcome measures, can predict successful return to sports and quality of life in athletes (age 16-55) after shoulder dislocation. The main research questions are: * Can an Upper Extremity Physical Performance Test Battery predict successful return to sports (= return to pre-injury sports level) in athletes after shoulder stabilization procedure * Can an Upper Extremity Physical Performance Test Battery predict the quality of life in athletes after shoulder stabilization procedure Participants will: * Fill out questionnaires pre-operatively * Fill out the SIRSI questionnaire throughout the rehabilitation * Undergo a testing battery in the return to sport phase, including physical performance tests, analytical tests and patient-reported outcome measures * Fill out questionnaires every 3 months after return to sports, up to 1 year.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other University Ghent trials

Trials by the same sponsor.

NCT07398053 — General Practitioner & Pharmacist Support for Discontinuing Long-term Antidepressants in Clinically Stable Patients · NA · not yet recruiting
NCT07343258 — Pilot Study on Follow-Up of (Acutely) Suicidal Individuals From the Flemish Suicide Helpline · NA · recruiting
NCT07091071 — Evaluation of the CochSyn Device in Clinical Practice · NA · completed
NCT07259408 — Co-creation of Tools for People in Detention With Suicidal Thoughts and/or Behavior · recruiting
NCT07176156 — Evaluation of the Quality of Chat Conversations With the Suicide Helpline Zelfmoordlijn 1813 · not yet recruiting

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT07115225 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University Ghent
Last refreshed: 11 August 2025

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07115225.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing